Role of Neurocellular Endoplasmic Reticulum Stress Response in Alzheimer's Disease and Related Dementias Risk.


Journal

Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097

Informations de publication

Date de publication:
28 Apr 2024
Historique:
received: 05 04 2024
revised: 24 04 2024
accepted: 26 04 2024
medline: 25 5 2024
pubmed: 25 5 2024
entrez: 25 5 2024
Statut: epublish

Résumé

Currently, more than 55 million people around the world suffer from dementia, and Alzheimer's Disease and Related Dementias (ADRD) accounts for nearly 60-70% of all those cases. The spread of Alzheimer's Disease (AD) pathology and progressive neurodegeneration in the hippocampus and cerebral cortex is strongly correlated with cognitive decline in AD patients; however, the molecular underpinning of ADRD's causality is still unclear. Studies of postmortem AD brains and animal models of AD suggest that elevated endoplasmic reticulum (ER) stress may have a role in ADRD pathology through altered neurocellular homeostasis in brain regions associated with learning and memory. To study the ER stress-associated neurocellular response and its effects on neurocellular homeostasis and neurogenesis, we modeled an ER stress challenge using thapsigargin (TG), a specific inhibitor of sarco/endoplasmic reticulum Ca

Identifiants

pubmed: 38790197
pii: genes15050569
doi: 10.3390/genes15050569
pii:
doi:

Substances chimiques

Protein Serine-Threonine Kinases EC 2.7.11.1
Endoribonucleases EC 3.1.-
Thapsigargin 67526-95-8
ERN1 protein, human EC 2.7.11.1
eIF-2 Kinase EC 2.7.11.1
EIF2AK3 protein, human EC 2.7.11.1
Activating Transcription Factor 6 0
ATF6 protein, human 0
X-Box Binding Protein 1 0
DDIT3 protein, human 0
Transcription Factor CHOP 147336-12-7

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIH HHS
ID : P01 HL045522
Pays : United States
Organisme : Valley Baptist Legacy Foundation
ID : 510000000
Organisme : NIH HHS
ID : U54 HG013247
Pays : United States
Organisme : NIH HHS
ID : RM1 GM149403
Pays : United States
Organisme : NIH HHS
ID : P30 AG066546
Pays : United States
Organisme : NIH HHS
ID : C06 RR020547
Pays : United States

Auteurs

Miriam Aceves (M)

Division of Human Genetics and South Texas Diabetes and Obesity Institute, University of Texas Rio Grande Valley School of Medicine, McAllen, TX 78504, USA.

Jose Granados (J)

Division of Human Genetics and South Texas Diabetes and Obesity Institute, University of Texas Rio Grande Valley School of Medicine, McAllen, TX 78504, USA.

Ana C Leandro (AC)

Division of Human Genetics and South Texas Diabetes and Obesity Institute, University of Texas Rio Grande Valley School of Medicine, Brownsville, TX 78520, USA.

Juan Peralta (J)

Division of Human Genetics and South Texas Diabetes and Obesity Institute, University of Texas Rio Grande Valley School of Medicine, Brownsville, TX 78520, USA.

David C Glahn (DC)

Department of Psychiatry, Boston Children's Hospital and Harvard Medical School, Boston, MA 02115, USA.

Sarah Williams-Blangero (S)

Division of Human Genetics and South Texas Diabetes and Obesity Institute, University of Texas Rio Grande Valley School of Medicine, Brownsville, TX 78520, USA.

Joanne E Curran (JE)

Division of Human Genetics and South Texas Diabetes and Obesity Institute, University of Texas Rio Grande Valley School of Medicine, Brownsville, TX 78520, USA.

John Blangero (J)

Division of Human Genetics and South Texas Diabetes and Obesity Institute, University of Texas Rio Grande Valley School of Medicine, Brownsville, TX 78520, USA.

Satish Kumar (S)

Division of Human Genetics and South Texas Diabetes and Obesity Institute, University of Texas Rio Grande Valley School of Medicine, McAllen, TX 78504, USA.

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Classifications MeSH